Women's Health Publications
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Panel Discussion: How ctDNA Testing is Informing the Management of Patients With GI Cancer
Our experts will review real-world case studies showing when and where ctDNA can help inform shared decision-making.
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Validation of an Enhanced Version of a Single- Nucleotide Polymorphism-Based Noninvasive Prenatal Test for Detection of Fetal Aneuploidies
Ryan A, Hunkapiller N, Banjevic M, et al. Fetal Diagn Ther 2016
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Informatics-based, highly accurate, noninvasive prenatal paternity testing
Ryan A, Baner J, Demko Z, et al. Genet Med 2013
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Letter to the Editor by Megan Hall in response to Munne S.
Saucier J, Merrion K, Mash J, et al. Current Genomics 2013
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Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphismebased noninvasive prenatal test
Curnow KJ, Wilkins-Haug L, Ryan A, et al. Am J Obstet Gynecol 2015
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Validation of a Single-Nucleotide Polymorphism-Based Non-Invasive Prenatal Test in Twin Gestations: Determination of Zygosity, Individual Fe
Norwitz ER, McNeill G, Kalyan A, et al. Journal of Clinical Medicine 2019
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Signatera Publications
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De novo HRAS gene mutation associated with Costello syndrome identified by non-invasive cell-free fetal DNA screening
Nwakalor C, Said-Delgado S, Krinshpun S, et al. Prenatal Diagnosis 2020
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Re: Clinical experience across the fetal-fraction spectrum of a non-invasive prenatal screening approach with low test-failure rate
Jelsema R, Demko ZP, Billing, PR. Ultrasound Obstet Gynecol. 2020
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Estimating the relative frequency of leukodystrophies and recommendations for carrier screening in the era of next-generation sequencing
Schmidt JL, Pizzino A, Nicholl J et al. American Journal of Medical Genetics Part A
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Primary cell-free DNA screening or contingent screening for the common trisomies: a response
Dar P, Norton ME. American Journal of Obstetrics and Gynecology 2022
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Performance of noninvasive prenatal screening for 22q11.2 deletion syndrome in the SMART study
Dar P, Norton ME. American Journal of Obstetrics and Gynecology 2022
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ProActive
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Why Cell‐Free DNA Can Be a “Game Changer” for Lung Allograft Monitoring for Rejection and Infection
Rosenheck JP, Keller BC, Fehringer G, et al. Curr Pulmonol Rep. 2022
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Letter to the Editors: Performance of Donor-derived Cell-free DNA Assays in Kidney Transplant Patients
Altug Y, Demko ZP, Ryan A. Letter to the Editors - Transplantation. 2020
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Using both the Fraction and Quantity of Donor-Derived Cell-Free DNA to Detect Kidney Allograft Rejection
Bunnapradist S, Homkrailas P, Ahmed E, et al. J Am Soc Nephrol 2021
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Single center experience comparing two clinically available donor derived cell free DNA tests and review of literature
Lum EL, Nieves-Borrero K, Homkrailas P, et al. Transplantation Reports. 2021
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Incorporation of Donor-derived Cell-free DNA Into Clinical Practice for Renal Allograft Management
Qazi Y, Patel A, Fajardo M, et al. Transplant Proc. 2021
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Preimplantation Genetic Testing for Kidney Disease-Related Genes: A Laboratory’s Experience
Chaperon JL, Wemmer NM, McKanna TA, et al. Am J Nephrol 2021
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